ENST00000367408.6:n.2535C>A
|
|
|
ENST00000367409.9:c.9248C>A
MANE Select
|
ENSP00000356379.4:p.Thr3083Lys
|
|
ENST00000680265.1:c.9470C>A
|
ENSP00000505384.1:p.Thr3157Lys
|
|
ENST00000680710.1:c.9248C>A
|
ENSP00000506676.1:p.Thr3083Lys
|
|
ENST00000294732.11:c.4493C>A
|
ENSP00000294732.7:p.Thr1498Lys
|
|
ENST00000367408.5:c.2243C>A
|
ENSP00000356378.1:p.Thr748Lys
|
|
ENST00000367409.8:c.9248C>A
|
ENSP00000356379.4:p.Thr3083Lys
|
|
ENST00000612785.1:c.3206C>A
|
ENSP00000479244.1:p.Thr1069Lys
|
|
NM_001206846.1:c.4493C>A
|
NP_001193775.1:p.Thr1498Lys
|
|
NM_018136.4:c.9248C>A
|
NP_060606.3:p.Thr3083Lys
|
|
NM_018136.5:c.9248C>A
MANE Select
|
NP_060606.3:p.Thr3083Lys
|
|
NM_001206846.2:c.4493C>A
|
NP_001193775.1:p.Thr1498Lys
|
|